MadSci Network: Biochemistry |
Hi
Candace,
As you
probably already know, alpha- and beta- nomenclature is used to distinguish
different stereoisomers of cyclical carbohydrate molecules (sugars). It is determined by whether the direction
that the hydroxyl group on the first carbon (relative to the endocyclical
oxygen - the oxygen in the ring) points axially (down, or alpha) or up
(equatorially, or beta).
If you
look
at the structure of Beta-D-Lactose, which is the form we mostly talk about
in
biology, you'll note that the glycosidic bond
between
galactose and glucose is a beta-bond...so the
galactose MUST be beta-galactose. However, the C1 carbon in glucose is far
away
from the glycosidic bond, so the glucose can be either alpha- or
beta-glucose. What's interesting is
that
a process called mutarotation of that carbon allows for alpha- and beta-
lactose
to convert back and forth from one another...at equilibrium, a molecule of
lactose in water at room temperature is 62.7% likely to be in the beta
form,
and 37.3% likely to occupy the alpha form.
I hope
this
has answered your question!
Billy.
PS - I
got most of the information for this answer from a very, very specific book
called "Dairy Chemistry and Biochemistry," which I checked out from my
school's library. Despite being
published in 1998 and purchased in 1999, I was still the very first person
to have ever checked out the book.
Fox and McSweeney. "Dairy Chemistry and
Biochemistry." Thompson Science.
1998. ISBN: 0-412-72000-
0
Try the links in the MadSci Library for more information on Biochemistry.